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Stephan Ehl

Showing results (61-70 of 239) with videos related to

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European Journal of Immunology|December 8, 2016
Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoireSandra Ammann, Kai Lehmberg, Udo Zur Stadt, et al.
Clinical Immunology (Orlando, Fla.)|April 21, 2019
Evaluating laboratory criteria for combined immunodeficiency in adult patients diagnosed with common variable immunodeficiencyCaroline von Spee-Mayer, Verena Koemm, Claudia Wehr, et al.
Journal of Virology|February 11, 2011
Both nonstructural proteins NS1 and NS2 of pneumonia virus of mice are inhibitors of the interferon type I and type III responses in vivoBritta Heinze, Stefanie Frey, Markus Mordstein, et al.
British Journal of Haematology|June 16, 2021
Primary haemophagocytic lymphohistiocytosis (Chédiak-Higashi Syndrome) triggered by acute SARS-CoV-2 infection in a six-week-old infantMatthias Lange, Tobias Linden, Hermann L Müller, et al.
European Journal of Immunology|May 19, 2020
Trigger-dependent differences determine therapeutic outcome in murine primary hemophagocytic lymphohistiocytosisRuth Gather, Peter Aichele, Nadja Goos, et al.
Pediatric Blood & Cancer|April 15, 2020
TIM-3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosisOliver Wegehaupt, Miriam Groß, Claudia Wehr, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2015
Preserved effector functions of human ORAI1- and STIM1-deficient neutrophilsRoland Elling, Baerbel Keller, Carl Weidinger, et al.
Pediatric Blood & Cancer|August 3, 2018
Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal diseaseMaximilian Heeg, Sandra Ammann, Christian Klemann, et al.
Clinical Immunology (Orlando, Fla.)|November 2, 2025
Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registryMaria Elena Maccari, Sven Kracker, Anita Chandra, et al.
The Journal of Allergy and Clinical Immunology|June 24, 2022
STAT3-confusion-of-function: Beyond the loss and gain dualismLorenzo Lodi, Laura Eva Faletti, Maria Elena Maccari, et al.
Pageof 24

Showing results (61-70 of 239) with videos related to

Sort By:
Pageof 24
European Journal of Immunology|December 8, 2016
Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoireSandra Ammann, Kai Lehmberg, Udo Zur Stadt, et al.
Clinical Immunology (Orlando, Fla.)|April 21, 2019
Evaluating laboratory criteria for combined immunodeficiency in adult patients diagnosed with common variable immunodeficiencyCaroline von Spee-Mayer, Verena Koemm, Claudia Wehr, et al.
Journal of Virology|February 11, 2011
Both nonstructural proteins NS1 and NS2 of pneumonia virus of mice are inhibitors of the interferon type I and type III responses in vivoBritta Heinze, Stefanie Frey, Markus Mordstein, et al.
British Journal of Haematology|June 16, 2021
Primary haemophagocytic lymphohistiocytosis (Chédiak-Higashi Syndrome) triggered by acute SARS-CoV-2 infection in a six-week-old infantMatthias Lange, Tobias Linden, Hermann L Müller, et al.
European Journal of Immunology|May 19, 2020
Trigger-dependent differences determine therapeutic outcome in murine primary hemophagocytic lymphohistiocytosisRuth Gather, Peter Aichele, Nadja Goos, et al.
Pediatric Blood & Cancer|April 15, 2020
TIM-3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosisOliver Wegehaupt, Miriam Groß, Claudia Wehr, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2015
Preserved effector functions of human ORAI1- and STIM1-deficient neutrophilsRoland Elling, Baerbel Keller, Carl Weidinger, et al.
Pediatric Blood & Cancer|August 3, 2018
Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal diseaseMaximilian Heeg, Sandra Ammann, Christian Klemann, et al.
Clinical Immunology (Orlando, Fla.)|November 2, 2025
Natural history of clinical manifestations in activated phosphoinositide 3-kinase δ syndrome (APDS): Time-to-event analyses using the European Society for Immunodeficiencies-APDS registryMaria Elena Maccari, Sven Kracker, Anita Chandra, et al.
The Journal of Allergy and Clinical Immunology|June 24, 2022
STAT3-confusion-of-function: Beyond the loss and gain dualismLorenzo Lodi, Laura Eva Faletti, Maria Elena Maccari, et al.
Pageof 24